Product code MHC— General Hospital
BD Intraosseous Infusion System
- Classification name
- Needle, Interosseous
- Device class
- Class 2
- Regulation
- 21 CFR 880.5570
- Advisory panel
- General Hospital
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code MHC
FDA has cleared devices under product code MHC between 2021 and 2022, filed by 2 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2022
- 2021
Top applicants under product code MHC
Recent clearances under product code MHC
Data sourced from openFDA. This site is unofficial and independent of the FDA.